ES516808A0 - A PROCEDURE FOR PREPARING ANTIBIOTICS FOR 1-AZABICICLO-3.2.0-HEPT-2-ENO. - Google Patents

A PROCEDURE FOR PREPARING ANTIBIOTICS FOR 1-AZABICICLO-3.2.0-HEPT-2-ENO.

Info

Publication number
ES516808A0
ES516808A0 ES516808A ES516808A ES516808A0 ES 516808 A0 ES516808 A0 ES 516808A0 ES 516808 A ES516808 A ES 516808A ES 516808 A ES516808 A ES 516808A ES 516808 A0 ES516808 A0 ES 516808A0
Authority
ES
Spain
Prior art keywords
hept
preparing
antibiotics
azabiciclo
eno
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
ES516808A
Other languages
Spanish (es)
Other versions
ES8402590A1 (en
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Gruppo Lepetit SpA
Original Assignee
Gruppo Lepetit SpA
Lepetit SpA
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Gruppo Lepetit SpA, Lepetit SpA filed Critical Gruppo Lepetit SpA
Publication of ES516808A0 publication Critical patent/ES516808A0/en
Publication of ES8402590A1 publication Critical patent/ES8402590A1/en
Expired legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D477/00—Heterocyclic compounds containing 1-azabicyclo [3.2.0] heptane ring systems, i.e. compounds containing a ring system of the formula:, e.g. carbapenicillins, thienamycins; Such ring systems being further condensed, e.g. 2,3-condensed with an oxygen-, nitrogen- or sulphur-containing hetero ring
    • C07D477/02—Preparation
    • C07D477/04—Preparation by forming the ring or condensed ring systems
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C67/00—Preparation of carboxylic acid esters
    • C07C67/30—Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group
    • C07C67/333—Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group by isomerisation; by change of size of the carbon skeleton
    • C07C67/343—Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D205/00—Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom
    • C07D205/02—Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom not condensed with other rings
    • C07D205/06—Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
    • C07D205/08—Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with one oxygen atom directly attached in position 2, e.g. beta-lactams

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Molecular Biology (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Hydrogenated Pyridines (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Cephalosporin Compounds (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)

Abstract

New beta -lactam acetic acid derivatives I <IMAGE> I wherein R represents alkyl, alkyl substituted with amino, protected amino, mono- or di-alkylamino, hydroxy, protected hydroxy or alkoxy, and alkenyl, and their salts are useful as intermediates for preparing 1-azabicyclo [3.2.0]hept-2-ene antibiotics II <IMAGE> II The process for preparing the beta -lactam acetic acid derivatives I as well as the overall process which starting from the acids I leads to the antibiotics II are also claimed.
ES516808A 1981-03-12 1982-10-25 New beta-lactam acetic acid derivatives, the process for preparing them, and their use as intermediates for 1-azabicyclo(3.2.0.)hept-2-ene antibiotics. Expired ES8402590A1 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB8107865 1981-03-12

Publications (2)

Publication Number Publication Date
ES516808A0 true ES516808A0 (en) 1984-02-01
ES8402590A1 ES8402590A1 (en) 1984-02-01

Family

ID=10520350

Family Applications (2)

Application Number Title Priority Date Filing Date
ES510336A Expired ES8308540A1 (en) 1981-03-12 1982-03-11 New beta-lactam acetic acid derivatives, the process for preparing them, and their use as intermediates for 1-azabicyclo(3.2.0.)hept-2-ene antibiotics.
ES516808A Expired ES8402590A1 (en) 1981-03-12 1982-10-25 New beta-lactam acetic acid derivatives, the process for preparing them, and their use as intermediates for 1-azabicyclo(3.2.0.)hept-2-ene antibiotics.

Family Applications Before (1)

Application Number Title Priority Date Filing Date
ES510336A Expired ES8308540A1 (en) 1981-03-12 1982-03-11 New beta-lactam acetic acid derivatives, the process for preparing them, and their use as intermediates for 1-azabicyclo(3.2.0.)hept-2-ene antibiotics.

Country Status (14)

Country Link
US (1) US4576746A (en)
EP (1) EP0060416B1 (en)
JP (1) JPS57159761A (en)
KR (1) KR880001847B1 (en)
AT (1) ATE21509T1 (en)
AU (1) AU548727B2 (en)
CA (1) CA1185244A (en)
DE (1) DE3272660D1 (en)
DK (1) DK103982A (en)
ES (2) ES8308540A1 (en)
IE (1) IE52609B1 (en)
IL (1) IL65232A (en)
PH (1) PH23415A (en)
ZA (1) ZA821252B (en)

Families Citing this family (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
HU187424B (en) * 1982-11-05 1986-01-28 Richter Gedeon Vegyeszeti Gyar Rt,Hu Process for preparing new azetidinyl-acetic acids
JPS60224672A (en) * 1984-04-23 1985-11-09 Sumitomo Chem Co Ltd Production of beta-lactam derivative
JPS62209079A (en) * 1986-03-11 1987-09-14 Sanraku Inc Disubstituted aminocarbapenam or such
JP2618271B2 (en) * 1989-04-26 1997-06-11 日本化薬株式会社 Crystal modification of magnesium mono-p-nitrobenzylmalonate and its preparation
CZ286267B6 (en) * 1992-09-18 2000-03-15 Merck & Co., Inc Process for preparing carbapenem intermediates and intermediates for making the process
US5516934A (en) * 1994-08-05 1996-05-14 Nippon Kayaku Kabushiki Kaisha Process for producing mono-P-nitrobenzyl malonate
US20040148868A1 (en) * 2003-02-05 2004-08-05 3M Innovative Properties Company Methods of making ceramics
WO2006061854A2 (en) * 2004-12-10 2006-06-15 Pharmed Medicare Private Limited CONTROL OF pH BY DIRECT ADDITION OF CARBONATES AND BICARBONATES DURING CONCENTRATION OF ORGANIC SOLVENT EXTRACTS OF 6- ACETYL- 4,1 ‘, 6' TRICHLOROGALACTOSUCROSE AND 4,1 ‘, 6' TRICHLOROGALACTOSUCROSE
PT2473605T (en) 2009-09-03 2018-05-28 Pfizer Vaccines Llc Pcsk9 vaccine
WO2011048583A1 (en) * 2009-10-23 2011-04-28 Ranbaxy Laboratories Limited Process for the preparation of carbapenem compounds
CN103483202B (en) * 2013-06-26 2015-01-21 华北水利水电大学 Preparation method of magnesium mono-p-nitrobenzyl malonate

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1570278A (en) * 1975-10-06 1980-06-25 Fujisawa Pharmaceutical Co O-substituted-2-azetidinone derivatives and the preparation thereof
US4138400A (en) * 1975-12-20 1979-02-06 Hoechst Aktiengesellschaft Omega-alkoxy derivatives of lactams
GB1584762A (en) * 1977-04-01 1981-02-18 Beecham Group Ltd Azabicycloheptenes
EP0017992A1 (en) * 1979-04-19 1980-10-29 Merck & Co. Inc. 2-Substituted-6-substituted-1-carbadethiapen-2-em-3-carboxylic acids, processes for preparing them, antibiotic pharmaceutical compositions containing same and process for preparing intermediates
US4290947A (en) * 1979-04-27 1981-09-22 Merck & Co., Inc. Process for the preparation of thienamycin and intermediates
US4312871A (en) * 1979-12-03 1982-01-26 Merck & Co., Inc. 6-, 1- And 2-substituted-1-carbadethiapen-2-em-3-carboxylic acids
US4262010A (en) * 1979-12-03 1981-04-14 Merck & Co., Inc. 6-(1-Hydroxyethyl)-2-(2-aminoethylthio)-1,1-disubstituted-1-carbadethiapen-2-em-3-carboxylic acids
US4269772A (en) * 1980-01-14 1981-05-26 Merck & Co., Inc. Synthesis of thienamycin via trans-3-carboxymethylene-4-carboxy-5-methyl-Δ2 -isoxazoline
US4287123A (en) * 1980-01-14 1981-09-01 Merck & Co., Inc. Synthesis of thienamycin via (3SR, 4RS)-3-((RS)-1-acyloxyethyl)-2-oxo-4-azetidineacetate
US4282148A (en) * 1980-01-14 1981-08-04 Merck & Co., Inc. Synthesis of thienamycin via esters of (3SR, 4RS)-3-[(SR)-1-hydroxyethyl]-β,2-dioxo-4-azetidinebutanoic acid

Also Published As

Publication number Publication date
US4576746A (en) 1986-03-18
IL65232A (en) 1986-01-31
ATE21509T1 (en) 1986-09-15
AU548727B2 (en) 1986-01-02
DK103982A (en) 1982-09-13
EP0060416B1 (en) 1986-08-20
ES8402590A1 (en) 1984-02-01
CA1185244A (en) 1985-04-09
KR880001847B1 (en) 1988-09-22
EP0060416A1 (en) 1982-09-22
DE3272660D1 (en) 1986-09-25
ZA821252B (en) 1983-01-26
IE820554L (en) 1982-09-12
JPS57159761A (en) 1982-10-01
PH23415A (en) 1989-08-07
IE52609B1 (en) 1987-12-23
ES510336A0 (en) 1983-09-01
IL65232A0 (en) 1982-05-31
KR830009020A (en) 1983-12-17
ES8308540A1 (en) 1983-09-01
AU8076582A (en) 1982-09-16

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Legal Events

Date Code Title Description
FD1A Patent lapsed

Effective date: 19981201